ClinVar Miner

List of variants in gene SCN8A reported as benign for not provided

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Total variants: 23
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HGVS dbSNP
NM_014191.4(SCN8A):c.1135-48C>T
NM_014191.4(SCN8A):c.1636-237G>A
NM_014191.4(SCN8A):c.2098A>T (p.Ile700Leu) rs187153231
NM_014191.4(SCN8A):c.2901+277T>C
NM_014191.4(SCN8A):c.3372+129A>G
NM_014191.4(SCN8A):c.3490+258G>A
NM_014191.4(SCN8A):c.3645+265A>G
NM_014191.4(SCN8A):c.3820-132G>T
NM_014191.4(SCN8A):c.3822C>T (p.Val1274=) rs187327463
NM_014191.4(SCN8A):c.3943-208G>A
NM_014191.4(SCN8A):c.395+262T>C
NM_014191.4(SCN8A):c.4122T>A (p.Thr1374=) rs115623439
NM_014191.4(SCN8A):c.4228-27C>T
NM_014191.4(SCN8A):c.4419+283C>T
NM_014191.4(SCN8A):c.4509T>C (p.Pro1503=) rs303815
NM_014191.4(SCN8A):c.4524+254T>C
NM_014191.4(SCN8A):c.4524+299G>A
NM_014191.4(SCN8A):c.4524+56A>G
NM_014191.4(SCN8A):c.5472C>A (p.Pro1824=) rs60637
NM_014191.4(SCN8A):c.5601G>A (p.Gln1867=) rs368449473
NM_014191.4(SCN8A):c.576C>T (p.Asp192=) rs4761829
NM_014191.4(SCN8A):c.5943_*2GAG[1] (p.Ter1981=) rs555793953
NM_014191.4(SCN8A):c.993-90_993-50del

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